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Selective capture of mesenchymal stem cells over fibroblasts and immune cells on E7-modified collagen substrates under flow circumstances†
Journal of Materials Chemistry B ( IF 7 ) Pub Date : 2017-12-04 00:00:00 , DOI: 10.1039/c7tb02812a
Xiaowen Zheng 1, 2, 3, 4, 5 , Xin Pan 1, 2, 3, 4, 5 , Qian Pang 1, 2, 3, 4, 5 , Chong Shuai 1, 2, 3, 4, 5 , Lie Ma 1, 2, 3, 4, 5 , Changyou Gao 1, 2, 3, 4, 5
Affiliation  

Recruitment of endogenous mesenchymal stem cells (MSCs) has become an attractive strategy for in situ tissue regeneration. However, it is of great importance to endow an implant with a specific affinity to MSCs, for many types of cells such as immune cells and fibroblasts can also be recruited. It has been demonstrated that E7 peptides have a specific affinity to MSCs, but their selectivity for MSCs when co-cultured with other cells, especially in flow conditions, has rarely been investigated. In this study, E7-modified collagen substrates were prepared using sulfosuccinimidyl 4-(N-maleimidomethyl) cyclohexane-1-carboxylate (sulfo-SMCC) as the coupling agent. The results of X-ray photoelectron spectroscopy (XPS) and quartz crystal microbalance (QCM) proved that the densities of the immobilized E7 peptides could be modulated by changing the amounts of sulfo-SMCC. The results of cell adhesion rate, adhesion area and adhesion force demonstrated that the immobilization of E7 peptides led to a significant enhancement of the adhesion of bone marrow-derived MSCs (BMSCs) compared to RAW264.7 cells and NIH3T3 cells. The selective adhesion was verified by co-culturing BMSCs with RAW264.7 cells and NIH3T3 cells, which indicated that higher proportions of BMSCs were adhered on the E7-immobilized substrates. By mimicking in vivo flow circumstances, the selective capture of BMSCs by the E7-modified substrates was revealed by a flow model. All these results suggest that E7 immobilization might be a promising strategy for an implant to achieve a better regeneration outcome by enhancing the affinity to the recruited MSCs.

中文翻译:

在流动情况下选择性捕获成纤维细胞之间的间充质干细胞和E7修饰的胶原基质上的免疫细胞

内源性间充质干细胞(MSCs)的招募已成为原位组织再生的一种有吸引力的策略。但是,赋予植入物对MSC特定的亲和力非常重要,因为还可以募集许多类型的细胞,例如免疫细胞和成纤维细胞。已经证明E7肽对MSC具有特异性亲和力,但是很少与其他细胞共培养时,特别是在流动条件下,其对MSC的选择性。在这项研究中,使用磺基琥珀酰亚胺4-(N-马来酰亚胺基甲基)环己烷-1-甲酸(磺基SMCC)作为偶联剂。X射线光电子能谱(XPS)和石英晶体微量天平(QCM)的结果证明,固定的E7肽的密度可以通过改变磺基-SMCC的量来调节。细胞粘附率,粘附面积和粘附力的结果表明,与RAW264.7细胞和NIH3T3细胞相比,E7肽的固定化显着增强了骨髓来源MSC(BMSC)的粘附性。通过将BMSC与RAW264.7细胞和NIH3T3细胞共培养来验证选择性粘附,这表明更高比例的BMSC粘附在固定了E7的底物上。通过模仿体内在流动情况下,通过流动模型揭示了E7修饰的底物对BMSC的选择性捕获。所有这些结果表明,E7固定化可能是植入物通过增强与募集的MSC的亲和力以获得更好的再生结果的一种有前途的策略。
更新日期:2017-12-04
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